- Open Access
A reduction in growth rate of Pseudomonas putida KT2442 counteracts productivity advances in medium-chain-length polyhydroxyalkanoate production from gluconate
© Follonier et al; licensee BioMed Central Ltd. 2011
Received: 25 February 2011
Accepted: 22 April 2011
Published: 22 April 2011
The substitution of plastics based on fossil raw material by biodegradable plastics produced from renewable resources is of crucial importance in a context of oil scarcity and overflowing plastic landfills. One of the most promising organisms for the manufacturing of medium-chain-length polyhydroxyalkanoates (mcl-PHA) is Pseudomonas putida KT2440 which can accumulate large amounts of polymer from cheap substrates such as glucose. Current research focuses on enhancing the strain production capacity and synthesizing polymers with novel material properties. Many of the corresponding protocols for strain engineering rely on the rifampicin-resistant variant, P. putida KT2442. However, it remains unclear whether these two strains can be treated as equivalent in terms of mcl-PHA production, as the underlying antibiotic resistance mechanism involves a modification in the RNA polymerase and thus has ample potential for interfering with global transcription.
To assess PHA production in P. putida KT2440 and KT2442, we characterized the growth and PHA accumulation on three categories of substrate: PHA-related (octanoate), PHA-unrelated (gluconate) and poor PHA substrate (citrate). The strains showed clear differences of growth rate on gluconate and citrate (reduction for KT2442 > 3-fold and > 1.5-fold, respectively) but not on octanoate. In addition, P. putida KT2442 PHA-free biomass significantly decreased after nitrogen depletion on gluconate. In an attempt to narrow down the range of possible reasons for this different behavior, the uptake of gluconate and extracellular release of the oxidized product 2-ketogluconate were measured. The results suggested that the reason has to be an inefficient transport or metabolization of 2-ketogluconate while an alteration of gluconate uptake and conversion to 2-ketogluconate could be excluded.
The study illustrates that the recruitment of a pleiotropic mutation, whose effects might reach deep into physiological regulation, effectively makes P. putida KT2440 and KT2442 two different strains in terms of mcl-PHA production. The differences include the onset of mcl-PHA production (nitrogen limitation) and the resulting strain performance (growth rate). It remains difficult to predict a priori where such major changes might occur, as illustrated by the comparable behavior on octanoate. Consequently, experimental data on mcl-PHA production acquired for P. putida KT2442 cannot always be extrapolated to KT2440 and vice versa, which potentially reduces the body of available knowledge for each of these two model strains for mcl-PHA production substantially.
Medium-chain-length polyhydroxyalkanoates (mcl-PHAs) are polyesters which combine the features of biodegradability, biocompatibility, and production from renewable carbon sources and as such constitute a promising alternative to petrol-based plastics . Mcl-PHAs are formed of monomers with 6 to 14 carbon atoms, in contrast to the short-chain-length polyhydroxyalkanoates (scl-PHAs) that contain 3 to 5 carbons per monomer. They are synthetized by Pseudomonads, principally under carbon excess conditions . Pseudomonas putida KT2440 and KT2442 belong to the best-known producers of mcl-PHA. They accumulate polymer from both PHA-related carbon sources (e. g. fatty acids) via β-oxidation and from PHA-unrelated carbon sources (e. g. sugars) via de novo fatty acid synthesis [2, 3]. P. putida KT2440, whose genome was sequenced a decade ago , originates from the toluene-degrading bacterium P. putida mt-2 isolated in Japan in 1960 by Hosakawa . P. putida KT2442 is a spontaneous rifampicin resistant mutant of P. putida KT2440 [6, 7] proposed to have a similar expression profile as P. putida KT2440 . Currently, much effort is spent on engineering these strains in order to increase their accumulation capacity, for instance by deletion of depolymerases , and in modifying the pathways involved in PHA synthesis so as to get polymers with modified compositions and improved material properties [10–13]. Knockout mutants are preferentially generated from the KT2442 strain as advantage can be taken from the rifampicin resistance to simplify the procedure. The mode of action of rifampicin consists of inhibiting bacterial growth by binding to the β-subunit of RNA polymerase and stopping mRNA elongation . Rifampicin-resistant mutants have an altered β-subunit of RNA polymerase [15, 16] and therefore their transcription profiles and physiology can be significantly affected.
Since P. putida KT2440 and KT2442 are mostly used for the production of mcl-PHA, we compared their performances on octanoate, a PHA-related carbon source, and on gluconate, a PHA-unrelated source. Citrate was used as control since it is a poor PHA-precursor (shown a posteriori, see Methods and Results). The two key parameters influencing PHA productivity (in g L-1 h-1) and as a result the production costs are the cell growth rate (in h-1) and the maximum PHA content (in wt %). The latter is especially important because a high PHA content additionally simplifies the down-stream process and thus decreases costs. Therefore, we performed shake flask experiments to determine these factors for the three growth substrates. It should be noted that the values reported here are not representative of optimized processes but qualitatively express if one strain shows better performances than the other one or not. The growth of P. putida KT2440 and KT2442 on gluconate was studied in more detail in a well-controlled bioreactor setting after discovering major physiological differences between the two strains.
In this work, we demonstrated that P. putida KT2440 and KT2442 produced mcl-PHA from the fatty acid octanoate with similar efficiency but that P. putida KT2442 had a strongly reduced productivity on gluconate because of a more than 3-fold smaller growth rate.
P. putida KT2442 exhibits reduced specific growth rate and production of mcl-PHA on gluconate compared to its parent KT2440
P. putida KT2442 can produce mcl-PHA from gluconate when the C/N ratio is increased
P. putida KT2442 PHA-free biomass decreases during nitrogen limiting growth on gluconate
Specific uptake and production rates of P. putida KT2440 and KT2442 cultivated in bioreactor on gluconate (21.2 g L-1)
qC(Gln) [g g h-1]
qC(2-KGln) [g g h-1]
qC* [g g h-1]
qN [g g h-1]
qC(Gln) [g g h-1]
qC(2-KGln) [g g h-1]
qPHA[g g h-1]
The conversion of gluconate into 2-ketogluconate is not affected in P. putida KT2442
In order to further investigate the nutrient uptake in P. putida KT2440 and KT2442, their specific carbon and nitrogen uptake rates were compared using the data from the batch experiments on gluconate in bioreactors. We defined the specific carbon consumption rate qC* as the specific rate at which carbon was utilized by the cells for respiration and production of biomass, and assumed that there was no accumulation of the substrate gluconate and of its metabolite 2-ketogluconate in the periplasm. Consequently, qC* could be calculated as the difference between the specific uptake rate of gluconate and the specific production rate of 2-ketogluconate (in g C). This expression could only be used until gluconate depletion. Afterwards, qC* was equivalent to the specific uptake rate of 2-ketogluconate (see the section Methods for the detailed calculations). Both the specific carbon and nitrogen uptake rates were 4-5 times lower for P. putida KT2442 than for P. putida KT2440 during the exponential phase (qC* = - 1.0 and - 0.2 g g-1 h-1, qN = - 0.062 and - 0.015 g g-1 h-1 for P. putida KT2440 and KT2442, respectively) (Table 1). This reduction fits well with the > 4-fold difference of growth rate between the strains, but whether the decreased uptake rates in P. putida KT2442 are the cause or the result of the slow growth remains unclear. In addition, the specific production rate of 2-ketogluconate of P. putida KT2442 was only half of the rate of P. putida KT2440 (qC(2-KGln) = + 0.5 and + 1.0 g g-1 h-1, respectively). The extent of gluconate converted into extracellular 2-ketogluconate was calculated from the rates qC(Gln) and qC(2-KGln) for P. putida KT2440 and KT2442. It was equal to 50% and >70%, respectively, which implies that the oxidation of gluconate was fully functional in P. putida KT2442.
Growth and PHA yields of P. putida KT2440 and KT2442 cultivated in bioreactor on gluconate (21.2 g L-1)
End exp. phase
YXr/C [g g-1]
YXr/N [g g-1]
End acc. phase
YXr/C [g g-1]
YXr/N [g g-1]
YPHA/C [g g-1]
How close are P. putida KT2440 and KT2442?
P. putida KT2440 and P. putida KT2442 have been extensively studied for the last 30 years, not only because of their interesting ability to accumulate mcl-PHA, but also as model organisms for laboratory studies and applications in bioremediation and biocatalysis [20, 21]. P. putida KT2440 and P. putida KT2442 are supposedly identical except regarding the rifampicin resistance. However, we observed different phenotypes between the two strains cultivated on gluconate: P. putida KT2442 displayed a reduced growth rate along with a lower growth yield for carbon and difficulties to cope with nitrogen limitation.
Rifampicin activity consists of inhibiting the bacterial DNA-dependent RNA polymerase by binding to it and stopping mRNA elongation . Rifampicin-resistant mutants produce RNA polymerases that have a slightly different β-subunit structure preventing the binding of rifampicin . Jatsenko et al. also showed recently that out of 167 rifampicin resistant mutants generated from P. putida PaW85 (P. putida mt-2 derivative cured of the TOL plasmid), all of them harbored the mutation of interest in the cluster I of rpoB gene . Because of the essential role of the RNA polymerase in gene transcription even slight modifications of its structure can have important and pleiotropic effects on the cell physiology. In particular, the regulatory nucleotide ppGpp was shown to bind at the interface between the β and β' subunits of E. coli RNA polymerase at 27 Å from the rifampicin binding site [22–25]. Therefore, modifications of RNA polymerase structure, even minor, could alter the binding of ppGpp with various consequences on the cell physiology. Indeed, ppGpp is a global transcription regulator mostly known for inhibiting growth and protein synthesis upon amino acid starvation but also involved in the regulation of many other functions [24, 26]. Besides, since P. putida KT2442 is a spontaneous mutant of P. putida KT2440 and not the result of a targeted procedure , the strain could harbor other mutations that may be made responsible for its poorer fitness. The determination of this (these) mutation(s) would require careful resequencing of KT2442. Nevertheless, a first step would be to determine whether the rifampicin resistance mutation is involved by reintroducing the wild-type rpoB gene from P. putida KT2440 in KT2442.
Gluconate transport and metabolism
Energy metabolism, nitrogen transport, and growth under nitrogen limitation
P. putida KT2440 and KT2442 grew with the same maximum specific growth rate on octanoate, indicating that the main energy production pathway (tricarboxylic acid cycle) worked properly. The slow growth rate observed for P. putida KT2442 on gluconate is therefore substrate-specific. However, P. putida KT2442 grew more slowly than P. putida KT2440 on citrate (μmax = 0.34 ± 0.02 h-1 and 0.54 ± 0.03 h-1, respectively). This could be the result of a problem with the expression of a citrate transporter or activator of citrate transport. An alternative explanation would be that the tricarboxylic acid cycle was only slightly slowed down in P. putida KT2442 so that it became growth limiting only when the cells were growing fast (e. g. on citrate) but not when they were growing more slowly (e. g. on octanoate).
When ammonium is present at high external concentrations as during the exponential phase, it enters the cytoplasm via unspecific diffusion of NH3 and does not require specific transporters. Therefore, the low specific uptake rate of nitrogen for P. putida KT2442 must be the consequence and not the cause of its slow growth rate. This conclusion is also supported by the fact that P. putida KT2442 and KT2440 had identical growth rates on octanoate.
P. putida KT2440 and KT2442 reacted differently with respect to nitrogen starvation. While the PHA-free biomass continued to increase a little and then remained constant for P. putida KT2440, it quickly decreased for P. putida KT2442 (Figure 4A and 4D). Also, the respiratory quotient of the latter strain progressively and significantly increased, whereas it remained stable for P. putida KT2440. This indicates a change of metabolism occurring for P. putida KT2442 as a result to nitrogen starvation. Although the gene expression in response to nitrogen limitation has been studied for P. putida KT2440 and KT2442 by Hervas et al. , it was not possible to formulate a reasonable hypothesis as to what caused this different behavior.
Nitrogen limitation is required for the accumulation of mcl-PHA from gluconate in P. putida KT2440 and KT2442
The data presented herein showed that nitrogen limitation was required to activate the production of mcl-PHA from gluconate in both P. putida KT2440 and KT2442. In contrast, we had observed previously that P. putida KT2440 cultivated on octanoate accumulated significant amounts of mcl-PHA even before nitrogen depletion (data not shown). Also, Sun et al. were able to produce more than 70 wt % of mcl-PHA from nonanoic acid in P. putida KT2440 without nitrogen limitation. Therefore, the requirement of a nutrient limitation to produce mcl-PHA seems to be substrate-dependent. As mentioned above, the synthesis of mcl-PHA by P. putida involves two different pathways depending on the precursor. Unrelated carbon sources such as gluconate are converted into polymer via de novo fatty acid synthesis and the intervention of the 3-hydroxy-acyl carrier protein (ACP)-CoA transacylase PhaG , whereas alkanes and fatty acids are channeled through the β-oxidation pathway . The origin for the need or not of nitrogen limitation may thus be linked to enzymes belonging to these pathways. Indeed, the enzyme PhaG was shown to be overexpressed under nitrogen starvation in P. putida KT2440 and KT2442 . However, other control systems may be involved as well.
This work shows substantial differences of physiology between the two closely related P. putida KT2440 and KT2442 upon growth on gluconate. A strong reduction of specific growth rate was observed for P. putida KT2442 as well as a smaller growth yield on carbon and difficulties to cope with nitrogen starvation. P. putida KT2442 is often preferred over P. putida KT2440 to generate metabolically engineered organisms with enhanced production of mcl-PHA because the procedure is simplified by the rifampicin resistance [17, 35]. However, the productivity of mcl-PHA - which is correlated to its cost - depends not only on the polymer content in the cells but also on their growth rate. Thus, the benefits of an increase in polymer accumulation from carbohydrates by metabolic engineering would be counteracted by a slow growth rate if P. putida KT2442 was used as host instead of P. putida KT2440.
Strains and media
The strains used in this study are P. putida KT2440 (own lab stock) and its rifampicin resistant derivative P. putida KT2442  which was kindly provided by M. A. Prieto (CIB, Madrid, Spain). The slow growth rate of P. putida KT2442 on gluconate was verified with a strain from our stock that originates from the lab of B. Witholt (ETHZ, Zurich, Switzerland).
The mineral medium used for the flask experiments was a modified medium E2  with a reduced concentration of nitrogen (0.064 g N L-1). It was supplemented with either sodium octanoate (1.66 g L-1), sodium gluconate (2.91 g L-1) or trisodium citrate dihydrate (3.92 g L-1) as carbon source. Thus, the three media had the same carbon concentration (0.96 g C L-1) and the same C/N ratio (15 g g-1).
The medium for the batch cultivations in bioreactor had the following composition: 4.8 g L-1 NaNH4PO4·4H2O (0.32 g N L-1), 21.2 g L-1 sodium gluconate (7.2 g C L-1), 3.7 g L-1 KH2PO4, 9.6 g L-1 K2HPO4, 0.03 g L-1 CaCl2·2H2O, 0.8 g L-1 EDTANa·2H2O, 1 g L-1 MgSO4·7H2O, 0.28 g L-1 FeSO4·7H2O and 2 mL L-1 of the following trace element solution: 12.22 g MnCl2·4H2O, 1.27 CoCl2·6H2O, 2.0 g CuCl2·2H2O, 7.5 g ZnSO4·7H2O, 0.5 g Na2MoO4·2H2O dissolved in 1 L HCl (1M). This medium had a C/N ratio of 22.5 g g-1 and was more concentrated to achieve higher cell density.
Shake flask experiments
Single colonies of the respective strains P. putida KT2440 and KT2442 were picked from a freshly streaked Luria-Bertani (LB) agar plate and grown overnight in LB medium at 30°C and 150 rpm. Three mL of these cultures were washed with mineral medium and used to inoculate 150 mL of each culture media (citrate, gluconate, and octanoate). The cultivation experiments were performed in 500 mL flasks with baffles shaken at 30°C and 150 rpm. The growth of each strain was studied in duplicates. Independent growth experiments were repeated in case of unexpected results; each time the first results were confirmed. At the end of the growth experiments, the biomass was collected for PHA analysis. The maximal specific growth rates and mcl-PHA contents were averaged from 2-4 values.
Fermentations in bioreactor
The fermentations in bioreactor were performed in a 16 L bioreactor (L1523, Bioengineering, Wald, Switzerland) with a starting volume of 11 L. Inoculation was done with 250 mL of an exponentially growing culture in modified medium E . Sterile polypropylene glycol was added to the culture to reduce foaming if necessary. The reactor was aerated with air (0.54 and 0.50 vvm for KT2440 and KT2442, respectively) and agitation varied from 300 to 700 rpm in order to avoid oxygen limitation. The temperature was set to 30°C and the pH kept between 6.85 and 6.95 by automated addition of KOH (4 M) and H3PO4 (4 M). The reactor was equipped with probes for pH and pO2 (Mettler Toledo, Greifensee, Switzerland). The off-gas concentrations of oxygen and carbon dioxide were monitored with a gas analyzer (BlueSens, Herten, Germany). The batch medium was autoclaved in situ without EDTANa·2H2O, MgSO4·7H2O, FeSO4·7H2O and gluconate that were sterile-filtered (0.22 μm pore size Millex-GP filter, Millipore, Billerica, USA) into the reactor after cooling.
Biomass. The optical density at 600 nm (OD600) of the cell culture was measured with a spectrophometer (Spectronic Genesys 6, Thermo Electron Corp., UK) and cell dry weight (CDW) concentrations were determined as described by Hartmann et al. . Residual concentrations of substrate. The concentration of ammonium nitrogen (NH4-N) was assessed by spectrophotometry (Ammonium-Test Spectroquant 1.14752.0001, Merck, Darmstadt, Germany) and the total organic carbon (TOC) was analyzed with a TOC-Analyzer (model TOC-5050A, Shimadzu, Reinach, Switzerland). The concentrations of gluconate and 2-ketogluconate were determined by HPLC-MS (Agilent 1000 Series, Santa Clara, United States for the HPLC unit, and Bruker Daltonics esquire HCT, Bremen, Germany for the MS unit). The column used was a Gemini C18 250 mm × 4.60 mm and 5 μm particle size (Phenomenex, Torrance, United States) operated isocratically with 90% of solvent A (H2O and 0.1% HCOOH) and 10% of solvent B (CH3CH and 0.1% HCOOH) for 15 min with a flow rate of 0.5 mL min-1. Ionisation was performed by atmospheric pressure chemical ionisation (ACPI) in negative mode. Xylose was used as internal standard. PHA content and composition. The PHA production was characterized by gas chromatography (GC) after propylation of the monomers according to Furrer et al. . PHA contents lower than 5 wt % were considered to negligible and the detected monomers to arise from cell membrane components. Indeed no PHA could be extracted [39, 40] from the biomass of P. putida KT2440 cultivated on citrate with a C/N ratio of 15 g g-1 although 5.1 wt % "PHA" were detected by GC (data not shown).
Specific uptake and production rates
This equation implies that the PHA-free biomass (Xr) stays constant which was the case for P. putida KT2440 but not for P. putida KT2442. Therefore the average between the two extremes values was considered for the latter strain.
Growth and PHA yields
C(Gln): gluconate-based carbon concentration [g L-1]; C(2-KGln): 2-ketogluconate-based carbon concentration [g L-1]; CDW: cell dry weight [g L-1]; CPR: carbon dioxide production rate [mol L-1 h-1]; FG: gas flow [L h-1]; Gln: gluconate; 2-KGln: 2-ketogluconate; μmax: maximum specific growth rate [h-1]; NH4-N: ammonium nitrogen [g L-1]; OD600: optical density (of a cell culture) at 600 nm [-]; OUR: oxygen uptake rate [mol L-1 h-1]; mcl-PHA: medium-chain-length polyhydroxyalkanoate; scl-PHA: short-chain-length polyhydroxyalkanoate; q: specific uptake/production rate [g g-1 h-1]; TOC: total organic carbon [g L-1]; RQ: respiratory quotient [mol mol-1]; Vm: molar volume [L mol-1]; Vw: working volume [L]; Xr: PHA-free biomass [g L-1]; y: molar fraction; YXr/C: growth yield for carbon [g g-1]; YXr/N: growth yield for nitrogen [g g-1]; YPHA/C: PHA yield for carbon [g g-1].
0: initial; C*: carbon effectively consumed by the cells for respiration and: biomass production; C(Gln): carbon present in gluconate; C(2-KGln): carbon present in 2-ketogluconate; e: end of exponential phase; f: final; in: inlet gas to the bioreactor; out: outlet gas from the bioreactor.
We thank B. Witholt and M. A. Prieto for providing us with strains of P. putida KT2440 and/or KT2442, K. Kehl for technical assistance for GC analysis, M. Richter and K. Grieder for help with HPLC-MS. This work was supported by the Swiss National Science Foundation.
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